MX2017012558A - DERIVATIVES OF BILIAR ACID AS FXR / TGR5 AGONISTS AND METHODS FOR USE. - Google Patents
DERIVATIVES OF BILIAR ACID AS FXR / TGR5 AGONISTS AND METHODS FOR USE.Info
- Publication number
- MX2017012558A MX2017012558A MX2017012558A MX2017012558A MX2017012558A MX 2017012558 A MX2017012558 A MX 2017012558A MX 2017012558 A MX2017012558 A MX 2017012558A MX 2017012558 A MX2017012558 A MX 2017012558A MX 2017012558 A MX2017012558 A MX 2017012558A
- Authority
- MX
- Mexico
- Prior art keywords
- fxr
- methods
- derivatives
- tgr5 agonists
- biliar
- Prior art date
Links
- IGRCWJPBLWGNPX-UHFFFAOYSA-N 3-(2-chlorophenyl)-n-(4-chlorophenyl)-n,5-dimethyl-1,2-oxazole-4-carboxamide Chemical compound C=1C=C(Cl)C=CC=1N(C)C(=O)C1=C(C)ON=C1C1=CC=CC=C1Cl IGRCWJPBLWGNPX-UHFFFAOYSA-N 0.000 title abstract 2
- 102100025353 G-protein coupled bile acid receptor 1 Human genes 0.000 title abstract 2
- 101000857733 Homo sapiens G-protein coupled bile acid receptor 1 Proteins 0.000 title abstract 2
- 239000002253 acid Substances 0.000 title 1
- 239000000556 agonist Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 230000001404 mediated effect Effects 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 150000004677 hydrates Chemical class 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/575—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of three or more carbon atoms, e.g. cholane, cholestane, ergosterol, sitosterol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/58—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/005—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of only two carbon atoms, e.g. pregnane derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0055—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J41/00—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring
- C07J41/0033—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005
- C07J41/0088—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 containing unsubstituted amino radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J43/00—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton
- C07J43/003—Normal steroids having a nitrogen-containing hetero ring spiro-condensed or not condensed with the cyclopenta(a)hydrophenanthrene skeleton not condensed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J9/00—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane
- C07J9/005—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane containing a carboxylic function directly attached or attached by a chain containing only carbon atoms to the cyclopenta[a]hydrophenanthrene skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J51/00—Normal steroids with unmodified cyclopenta(a)hydrophenanthrene skeleton not provided for in groups C07J1/00 - C07J43/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Epidemiology (AREA)
- Endocrinology (AREA)
- Vascular Medicine (AREA)
- Emergency Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Transplantation (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Steroid Compounds (AREA)
Abstract
La presente invención provee compuestos representados por la Fórmula I o sales, estereoisómeros, solvatos, hidratos farmacéuticamente aceptables o combinaciones de estos: La invención también provee composiciones farmacéuticas que comprenden estos compuestos y métodos para usar estos compuestos en el tratamiento de afecciones o enfermedades mediadas por FXR o mediadas por TGR5.The present invention provides compounds represented by Formula I or pharmaceutically acceptable salts, stereoisomers, solvates, hydrates or combinations thereof: The invention also provides pharmaceutical compositions comprising these compounds and methods for using these compounds in the treatment of conditions or diseases mediated by FXR or mediated by TGR5.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562140927P | 2015-03-31 | 2015-03-31 | |
| US201662287267P | 2016-01-26 | 2016-01-26 | |
| PCT/US2016/025035 WO2016161003A1 (en) | 2015-03-31 | 2016-03-30 | Bile acid derivatives as fxr/tgr5 agonists and methods of use thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MX2017012558A true MX2017012558A (en) | 2018-04-20 |
| MX379579B MX379579B (en) | 2025-03-11 |
Family
ID=57007583
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2017012558A MX379579B (en) | 2015-03-31 | 2016-03-30 | BILE ACID DERIVATIVES AS FXR/TGR5 AGONISTS AND METHODS OF THEIR USE. |
Country Status (27)
| Country | Link |
|---|---|
| US (4) | US10457703B2 (en) |
| EP (1) | EP3277286B1 (en) |
| JP (1) | JP6785788B2 (en) |
| KR (1) | KR102681304B1 (en) |
| CN (1) | CN107427527B (en) |
| AU (1) | AU2016242861B2 (en) |
| CA (1) | CA2981503C (en) |
| CY (1) | CY1124404T1 (en) |
| DK (1) | DK3277286T3 (en) |
| ES (1) | ES2886766T3 (en) |
| HR (1) | HRP20211066T1 (en) |
| HU (1) | HUE054960T2 (en) |
| IL (1) | IL254288B (en) |
| LT (1) | LT3277286T (en) |
| MX (1) | MX379579B (en) |
| MY (1) | MY192135A (en) |
| NZ (1) | NZ735126A (en) |
| PH (1) | PH12017501586A1 (en) |
| PL (1) | PL3277286T3 (en) |
| PT (1) | PT3277286T (en) |
| RS (1) | RS62110B1 (en) |
| RU (1) | RU2712099C2 (en) |
| SG (2) | SG11201707263XA (en) |
| SI (1) | SI3277286T1 (en) |
| SM (1) | SMT202100593T1 (en) |
| WO (1) | WO2016161003A1 (en) |
| ZA (2) | ZA201707212B (en) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1948236B1 (en) | 2005-09-27 | 2021-03-03 | Special Water Patents B.V. | Methods and compositions for treatment of skin |
| AU2015343025A1 (en) | 2014-11-06 | 2017-06-08 | Enanta Pharmaceuticals, Inc. | Bile acid analogs an FXR/TGR5 agonists and methods of use thereof |
| WO2016086115A1 (en) | 2014-11-26 | 2016-06-02 | Enanta Pharmaceuticals, Inc. | Tetrazole derivatives of bile acids as fxr/tgr5 agonists and methods of use thereof |
| US10208081B2 (en) | 2014-11-26 | 2019-02-19 | Enanta Pharmaceuticals, Inc. | Bile acid derivatives as FXR/TGR5 agonists and methods of use thereof |
| MX2017006833A (en) | 2014-11-26 | 2018-02-13 | Enanta Pharm Inc | Bile acid analogs as fxr/tgr5 agonists and methods of use thereof. |
| JP6785788B2 (en) | 2015-03-31 | 2020-11-18 | エナンタ ファーマシューティカルズ インコーポレイテッド | Bile acid derivatives as FXR / TGR5 agonists and how to use them |
| WO2017129125A1 (en) * | 2016-01-28 | 2017-08-03 | 正大天晴药业集团股份有限公司 | Steroid derivative fxr agonist |
| US10364267B2 (en) | 2016-02-23 | 2019-07-30 | Enanta Pharmaceuticals, Inc. | Deuterated bile acid derivatives as FXR/TGR5 agonists and methods of use thereof |
| US10323061B2 (en) | 2016-02-23 | 2019-06-18 | Enanta Pharmaceuticals, Inc. | Heteroaryl containing bile acid analogs as FXR/TGR5 agonists and methods of use thereof |
| US10323060B2 (en) | 2016-02-23 | 2019-06-18 | Enanta Pharmaceuticals, Inc. | Benzoic acid derivatives of bile acid as FXR/TGR5 agonists and methods of use thereof |
| EA038580B9 (en) * | 2016-05-18 | 2021-10-05 | Чиа Тай Тяньцин Фармасьютикал Груп Ко., Лтд. | Steroid derivative fxr agonist |
| CA3045023A1 (en) | 2016-11-29 | 2018-06-07 | Enanta Pharmaceuticals, Inc. | Process for preparation of sulfonylurea bile acid derivatives |
| CN108218946B (en) * | 2016-12-15 | 2021-04-16 | 宁波百纳西药业有限公司 | A kind of deoxycholic acid compound, its preparation method and application |
| CN108218945B (en) * | 2016-12-15 | 2021-05-28 | 宁波百纳西药业有限公司 | Deoxycholic acid derivative, its preparation method, pharmaceutical composition and use |
| US10472386B2 (en) | 2017-02-14 | 2019-11-12 | Enanta Pharmaceuticals, Inc. | Bile acid derivatives as FXR agonists and methods of use thereof |
| JP7136802B2 (en) * | 2017-04-07 | 2022-09-13 | エナンタ ファーマシューティカルズ インコーポレイテッド | Process for the preparation of sulfonyl carbamate bile acid derivatives |
| AU2018288883B2 (en) | 2017-06-23 | 2022-06-02 | Intercept Pharmaceuticals, Inc. | Methods and intermediates for the preparation of bile acid derivatives |
| CN110869381B (en) * | 2017-07-26 | 2021-11-19 | 正大天晴药业集团股份有限公司 | Preparation method of steroid derivative FXR agonist |
| GB201812382D0 (en) | 2018-07-30 | 2018-09-12 | Nzp Uk Ltd | Compounds |
| US20220241376A1 (en) | 2019-07-18 | 2022-08-04 | Enyo Pharma | Method for decreasing adverse-effects of interferon |
| PH12022550852A1 (en) | 2019-10-07 | 2023-05-03 | Kallyope Inc | Gpr119 agonists |
| CN114945361A (en) | 2020-01-15 | 2022-08-26 | 法国国家卫生及研究医学协会 | Use of FXR agonists for the treatment of hepatitis delta virus infection |
| CA3173731A1 (en) | 2020-02-28 | 2021-09-02 | Kallyope, Inc. | Gpr40 agonists |
| US12215127B2 (en) | 2020-04-17 | 2025-02-04 | Cornell University | Compositions and methods for profiling of gut microbiota-associated bile salt hydrolase (BSH) activity |
| US12030912B2 (en) * | 2020-05-15 | 2024-07-09 | Brigham Young University | Cationic steroidal antimicrobial compounds with urethane linkages |
| KR20230012597A (en) | 2020-05-19 | 2023-01-26 | 칼리오페, 인크. | AMPK activator |
| AU2021297323A1 (en) | 2020-06-26 | 2023-02-16 | Kallyope, Inc. | AMPK activators |
| US20240100125A1 (en) | 2021-01-14 | 2024-03-28 | Enyo Pharma | Synergistic effect of a fxr agonist and ifn for the treatment of hbv infection |
| EP4329761A1 (en) | 2021-04-28 | 2024-03-06 | ENYO Pharma | Strong potentiation of tlr3 agonists effects using fxr agonists as a combined treatment |
| WO2023288123A1 (en) | 2021-07-16 | 2023-01-19 | Interecept Pharmaceuticals, Inc. | Methods and intermediates for the preparation of 3.alpha.,7.alpha.,11.beta.-trihydroxy-6.alpha.-ethyl-5.beta.-cholan-24-oic acid |
Family Cites Families (144)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1592791A (en) | 1977-01-07 | 1981-07-08 | Radiochemical Centre Ltd | Selenium- or tellurium-containing bile acids and derivatives thereof |
| EP0243449A1 (en) | 1985-10-18 | 1987-11-04 | The Upjohn Company | Cyclic hydrocarbons with an aminoalkyl sidechain |
| US5571809A (en) | 1989-04-20 | 1996-11-05 | Boehringer Ingelheim Pharmaceuticals, Inc. | The treatment of HIV-1 infection using certain pyridodiazepines |
| IT1255449B (en) | 1992-06-30 | 1995-10-31 | Fabio Berlati | USE OF NOR- AND HOMO-DERIVATIVES OF BILE ACIDS AS DRUGS ABSORPTION PROMOTERS. |
| IT1255485B (en) | 1992-08-04 | 1995-11-06 | Erregierre Ind Chim | PROCESS TO PREPARE GLYCINE CONJUGATED BILIARY ACIDS AND RELATED THERAPEUTIC COMPOSITIONS FOR THE TREATMENT OF HEPATIC INSUFFICIENCY |
| TW289020B (en) | 1993-05-08 | 1996-10-21 | Hoechst Sktiengesellschaft | |
| TW289757B (en) | 1993-05-08 | 1996-11-01 | Hoechst Ag | |
| US5541348A (en) * | 1994-03-10 | 1996-07-30 | National Research Council Of Canada | Bile acids for biological and chemical applications and processes for the production thereof |
| ATE372966T1 (en) | 1994-03-25 | 2007-09-15 | Isotechnika Inc | IMPROVED EFFECTIVENESS OF DRUGS THROUGH DEUTERATION |
| US5646316A (en) | 1994-04-08 | 1997-07-08 | Osteoarthritis Sciences, Inc. | Bile acid inhibitors of metalloproteinase enzymes |
| JPH1160594A (en) | 1997-08-25 | 1999-03-02 | Sankyo Co Ltd | Bile acid derivative |
| JP3865890B2 (en) * | 1997-09-30 | 2007-01-10 | 富士フイルムホールディングス株式会社 | Positive photosensitive composition |
| CA2356887A1 (en) | 1998-12-23 | 2000-06-29 | Glaxo Group Limited | Assays for ligands for nuclear receptors |
| US20020132223A1 (en) | 1999-03-26 | 2002-09-19 | City Of Hope | Methods for modulating activity of the FXR nuclear receptor |
| CA2372150C (en) | 1999-04-30 | 2011-08-30 | The Regents Of The University Of Michigan | Therapeutic applications of pro-apoptotic benzodiazepines |
| US20020098999A1 (en) * | 2000-10-06 | 2002-07-25 | Gallop Mark A. | Compounds for sustained release of orally delivered drugs |
| US6992076B2 (en) * | 2000-10-06 | 2006-01-31 | Xenoport, Inc. | Bile-acid derived compounds for providing sustained systemic concentrations of drugs after oral administration |
| JP4021327B2 (en) | 2001-03-12 | 2007-12-12 | インターセプト ファーマスーティカル インコーポレイテッド | Steroids as agonists for FXR |
| DE60131967D1 (en) | 2001-08-13 | 2008-01-31 | Phenex Pharmaceuticals Ag | Nr1h4 nuclear receptor binding compounds |
| AU2003228485A1 (en) | 2002-04-12 | 2003-10-27 | The University Of Chicago | Farnesoid x-activated receptor agonists |
| ITMI20021080A1 (en) | 2002-05-21 | 2003-11-21 | Marcello Izzo | PHARMACEUTICAL ASSOCIATIONS FOR TOPICAL USE BASED ON CHELATES OF THE METAL PROTEASIS FERROINHIBITORS AND FACTOR XIII FOR THE TREATMENT OF |
| WO2004046162A2 (en) | 2002-11-14 | 2004-06-03 | The Scripps Research Institute | Non-steroidal fxr agonists |
| US7319109B2 (en) | 2002-11-22 | 2008-01-15 | Smith Kline Beecham Corporation | Farnesoid X receptor agonists |
| WO2005054213A1 (en) | 2003-12-02 | 2005-06-16 | Shionogi & Co., Ltd. | Isoxazole derivative having agonistic activity against peroxisome proliferator-activated receptor |
| EP1568706A1 (en) | 2004-02-26 | 2005-08-31 | Intercept Pharmaceuticals, Inc. | Novel steroid agonist for FXR |
| HUE032928T2 (en) | 2004-03-12 | 2017-11-28 | Intercept Pharmaceuticals Inc | Treatment of fibrosis using Fxr ligands |
| ITMI20050912A1 (en) | 2005-05-19 | 2006-11-20 | Erregierre Spa | PROCESS OF PREPARATION OF ACIDS 3-A-YA (B) -DIDROSSI-6-A (B) -ALCHIL-5B-COLANICI |
| WO2007076260A2 (en) | 2005-12-19 | 2007-07-05 | Smithkline Beecham Corporation | Farnesoid x receptor agonists |
| AU2007209928B2 (en) | 2006-01-30 | 2013-03-28 | Exelixis, Inc. | 4-aryl-2-amino-pyrimidines or 4-aryl-2-aminoalkyl-pyrimidines as JAK-2 modulators and pharmaceutical compositions containing them |
| CN102145005A (en) | 2006-02-01 | 2011-08-10 | 杨百翰大学 | Cationic steroid antimicrobial compositions and methods of use |
| US7863302B2 (en) | 2006-02-03 | 2011-01-04 | Eli Lilly And Company | Compounds and methods for modulating FX-receptors |
| WO2007095174A2 (en) | 2006-02-14 | 2007-08-23 | Intercept Pharmaceuticals, Inc. | Bile acid derivatives as fxr ligands for the prevention or treatment of fxr-mediated diseases or conditions |
| US20090131384A1 (en) | 2006-03-22 | 2009-05-21 | Syndexa Pharmaceuticals Corporation | Compounds and methods for treatment of disorders associated with er stress |
| DK2029547T3 (en) | 2006-05-24 | 2010-07-26 | Lilly Co Eli | FXR agonists |
| PE20080344A1 (en) | 2006-06-27 | 2008-06-09 | Sanofi Aventis | 8-AZABICYCLE COMPOUNDS [3.2.1] OCT-8-IL-1,2,3,4-TETRAHYDROQUINOLINE SUBSTITUTED AS INHIBITORS 11B-HSD1 |
| DK2040713T3 (en) | 2006-06-27 | 2014-09-29 | Intercept Pharmaceuticals Inc | BILIC ACID DERIVATIVES AS FXR LIGANDS FOR THE PREVENTION OR TREATMENT OF FXR-MEDIATED DISEASES OR CONDITIONS |
| CA2657716A1 (en) | 2006-07-17 | 2008-01-24 | Novartis Ag | Cholanic acid amides |
| CN101535303B (en) | 2006-08-15 | 2012-07-18 | 诺瓦提斯公司 | Heterocyclic compounds suitable for the treatment of diseases related to elevated lipid level |
| EP1894928A1 (en) | 2006-08-29 | 2008-03-05 | PheneX Pharmaceuticals AG | Heterocyclic fxr binding compounds |
| EP1894924A1 (en) | 2006-08-29 | 2008-03-05 | Phenex Pharmaceuticals AG | Heterocyclic FXR binding compounds |
| US20100063697A1 (en) | 2006-09-15 | 2010-03-11 | Volvo Lastvagnar Ab | Method for adapting an automatic mechanical transmission on a heavy vehicle |
| CL2007003035A1 (en) | 2006-10-24 | 2008-05-16 | Smithkline Beechman Corp | COMPOUNDS DERIVED FROM ISOXAZOL REPLACED, FARNESOID X RECEIVER AGONISTS; PREPARATION PROCEDURE; PHARMACEUTICAL COMPOSITION THAT UNDERSTANDS IT; AND USE OF THE COMPOUND IN THE TREATMENT OF OBESITY, DIABETES MELLITUS, FIBROSIS IN ORGANS, |
| EP1918281A1 (en) | 2006-11-02 | 2008-05-07 | Laboratorios del Dr. Esteve S.A. | Phenylamino-substituted piperidine compounds, their preparation and use as medicaments |
| JP2010513458A (en) | 2006-12-19 | 2010-04-30 | ファイザー・プロダクツ・インク | Nicotinamide derivatives as inhibitors of H-PGDS and their use to treat prostaglandin D2-mediated diseases |
| EA017714B1 (en) * | 2007-01-19 | 2013-02-28 | Интерсепт Фармасьютикалз, Инк. | Tgr5 modulators and methods of use thereof |
| EP1947108A1 (en) | 2007-01-19 | 2008-07-23 | Intercept Pharmaceuticals, Inc. | TGR5 modulators and methods of use thereof |
| US20100158992A1 (en) | 2007-03-15 | 2010-06-24 | Schering Corporation | Piperazine-substituted pyridazinone derivatives useful as glucan synthase inhibitors |
| BRPI0812521A2 (en) | 2007-06-13 | 2015-06-23 | Glaxosmithkline Llc | Compound, pharmaceutical composition, method for treating disease in a mammal, process for preparing a compound, and use of a compound |
| KR20100044810A (en) | 2007-07-02 | 2010-04-30 | 글락소스미스클라인 엘엘씨 | Farnesoid x receptor agonists |
| TW200906823A (en) | 2007-07-16 | 2009-02-16 | Lilly Co Eli | Compounds and methods for modulating FXR |
| US8338628B2 (en) | 2007-08-28 | 2012-12-25 | City Of Hope | Method of synthesizing alkylated bile acid derivatives |
| EP3293195A1 (en) | 2007-09-06 | 2018-03-14 | OHR Pharmaceutical, Inc. | Compounds for use in treating diabetes |
| US20090163474A1 (en) | 2007-10-19 | 2009-06-25 | Wyeth | FXR Agonists for the Treatment of Nonalcoholic Fatty Liver and Cholesterol Gallstone Diseases |
| KR101239008B1 (en) * | 2008-03-31 | 2013-03-04 | 한양대학교 산학협력단 | Bilic acid derivatives and their applications |
| EP2110374A1 (en) | 2008-04-18 | 2009-10-21 | Merck Sante | Benzofurane, benzothiophene, benzothiazol derivatives as FXR modulators |
| EP2128158A1 (en) | 2008-05-26 | 2009-12-02 | Phenex Pharmaceuticals AG | Heterocyclic cyclopropyl-substituted FXR binding compounds |
| EP2324046B1 (en) | 2008-07-30 | 2014-09-03 | Intercept Pharmaceuticals, Inc. | Tgr5 modulators and methods of use thereof |
| AR073920A1 (en) | 2008-10-23 | 2010-12-09 | Boehringer Ingelheim Int | UREA DERIVATIVES OF SUBSTITUTED NORTROPANS, DRUGS CONTAINING THESE COMPOUNDS, THEIR USE IN THE TREATMENT OF DISEASES MEDIATED BY THE INHIBITION OF THE 11BETA-HYDROXIESTEROID DISHYDROGENASE DISEASE AND PROCESS FOR PREPARATION. |
| KR20110119790A (en) | 2009-02-12 | 2011-11-02 | 엑셀리시스, 인코포레이티드 | Triazole and imidazole derivatives used as TVR5 agonists to treat diabetes and obesity |
| US8329904B2 (en) | 2009-05-12 | 2012-12-11 | Hoffmann-La Roche Inc. | Azacyclic derivatives |
| WO2011021645A1 (en) | 2009-08-19 | 2011-02-24 | 大日本住友製薬株式会社 | Bicyclic urea derivative or pharmacologically permitted salt thereof |
| EP2289883A1 (en) | 2009-08-19 | 2011-03-02 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
| ES2564318T3 (en) | 2009-11-05 | 2016-03-21 | Glaxosmithkline Llc | Benzodiazepine Bromodomain Inhibitor |
| JP2014500318A (en) | 2010-12-20 | 2014-01-09 | アイアールエム・リミテッド・ライアビリティ・カンパニー | Compositions and methods for modulating farnesoid X receptor |
| CU24152B1 (en) | 2010-12-20 | 2016-02-29 | Irm Llc | 1,2 OXAZOL-8-AZABICICLO [3,2,1] OCTANO 8 IL AS FXR MODULATORS |
| US20140039007A1 (en) | 2010-12-20 | 2014-02-06 | David C. Tully | Compositions and methods for modulating farnesoid x receptors |
| EP2545964A1 (en) | 2011-07-13 | 2013-01-16 | Phenex Pharmaceuticals AG | Novel FXR (NR1H4) binding and activity modulating compounds |
| US20130034536A1 (en) | 2011-08-04 | 2013-02-07 | Lumena Pharmaceuticals, Inc. | Bile Acid Recycling Inhibitors for Treatment of Pancreatitis |
| WO2013037482A1 (en) | 2011-09-15 | 2013-03-21 | Phenex Pharmaceuticals Ag | Farnesoid x receptor agonists for cancer treatment and prevention |
| US11154559B2 (en) | 2011-09-29 | 2021-10-26 | Ethicon Endo-Surgery, Inc. | Methods and compositions of bile acids |
| MX2014013150A (en) | 2012-05-01 | 2015-05-11 | Catabasis Pharmaceuticals Inc | Fatty acid conjugates of statin and fxr agonists; compositions and method of uses. |
| CN111228278A (en) | 2012-06-19 | 2020-06-05 | 英特塞普特医药品公司 | Preparation, use and solid forms of obeticholic acid |
| US9079935B2 (en) | 2012-08-13 | 2015-07-14 | The Board Of Regents Of The Nevada System Of Higher Education On Behalf Of The University Of Nevada, Las Vegas | Reducing risk of contracting Clostridium-difficile associated disease |
| WO2014036377A1 (en) * | 2012-08-31 | 2014-03-06 | Metselex | Methods of promoting cell viability |
| US9814733B2 (en) | 2012-12-31 | 2017-11-14 | A,arin Pharmaceuticals Ireland Limited | Compositions comprising EPA and obeticholic acid and methods of use thereof |
| US20140187633A1 (en) | 2012-12-31 | 2014-07-03 | Amarin Pharmaceuticals Ireland Limited | Methods of treating or preventing nonalcoholic steatohepatitis and/or primary biliary cirrhosis |
| US20140206657A1 (en) * | 2013-01-18 | 2014-07-24 | City Of Hope | Bile acid analog tgr5 agonists |
| PT3360881T (en) | 2013-05-14 | 2021-02-19 | Intercept Pharmaceuticals Inc | 11-hydroxyl-6-substituted-derivatives of bile acids and amino acid conjugates thereof as farnesoid x receptor modulators |
| WO2015017813A2 (en) | 2013-08-01 | 2015-02-05 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Inhibitors of the farnesoid x receptor and uses in medicine |
| PL3043865T3 (en) | 2013-09-11 | 2021-07-05 | Institut National De La Santé Et De La Recherche Médicale (Inserm) | Methods and pharmaceutical compositions for the treatment of hepatitis b virus infection |
| US20150112089A1 (en) | 2013-10-22 | 2015-04-23 | Metselex, Inc. | Deuterated bile acids |
| MX373721B (en) | 2014-05-29 | 2020-04-20 | Bar Pharmaceuticals S R L | CHOLANE DERIVATIVES FOR USE IN THE TREATMENT AND/OR PREVENTION OF DISEASES INVOLVING FXR AND TGR5/GPBAR1. |
| AU2015343025A1 (en) | 2014-11-06 | 2017-06-08 | Enanta Pharmaceuticals, Inc. | Bile acid analogs an FXR/TGR5 agonists and methods of use thereof |
| CN111944006B (en) | 2014-11-17 | 2021-12-17 | 正大天晴药业集团股份有限公司 | New 7-keto-6 beta-alkyl cholanic acid derivative in preparation of obeticholic acid and application thereof in medical field |
| MX2017006833A (en) | 2014-11-26 | 2018-02-13 | Enanta Pharm Inc | Bile acid analogs as fxr/tgr5 agonists and methods of use thereof. |
| WO2016086115A1 (en) | 2014-11-26 | 2016-06-02 | Enanta Pharmaceuticals, Inc. | Tetrazole derivatives of bile acids as fxr/tgr5 agonists and methods of use thereof |
| US20160176917A1 (en) | 2014-11-26 | 2016-06-23 | Enanta Pharmaceuticals, Inc. | Bile Acid Derivatives as FXR/TGR5 Agonists and Methods of Use Thereof |
| US10208081B2 (en) | 2014-11-26 | 2019-02-19 | Enanta Pharmaceuticals, Inc. | Bile acid derivatives as FXR/TGR5 agonists and methods of use thereof |
| EP3034499A1 (en) | 2014-12-17 | 2016-06-22 | Gilead Sciences, Inc. | Novel FXR (NR1H4) modulating compounds |
| EP3034501A1 (en) | 2014-12-17 | 2016-06-22 | Gilead Sciences, Inc. | Hydroxy containing FXR (NR1H4) modulating compounds |
| RU2017125365A (en) | 2014-12-18 | 2019-01-21 | Новартис Аг | Derivatives of azabicyclohexane as FXR agonists for use in the treatment of liver diseases and gastrointestinal diseases |
| US10246483B2 (en) | 2015-02-11 | 2019-04-02 | Enanta Pharmaceuticals, Inc. | Bile acid analogs as FXR/TGR5 agonists and methods of use thereof |
| TWI698430B (en) | 2015-02-13 | 2020-07-11 | 南北兄弟藥業投資有限公司 | Tricyclic compounds and uses thereof in medicine |
| JP6785788B2 (en) | 2015-03-31 | 2020-11-18 | エナンタ ファーマシューティカルズ インコーポレイテッド | Bile acid derivatives as FXR / TGR5 agonists and how to use them |
| CN106083978A (en) | 2015-04-28 | 2016-11-09 | 上海迪诺医药科技有限公司 | Sulfonyl amino carbonyl derivant, its pharmaceutical composition and application |
| WO2016173397A1 (en) | 2015-04-28 | 2016-11-03 | 上海翰森生物医药科技有限公司 | Cholic acid derivative, and preparation method and medical use thereof |
| TW201704251A (en) | 2015-04-29 | 2017-02-01 | 正大天晴藥業集團股份有限公司 | Chenodeoxycholic acid derivative |
| WO2016205475A2 (en) | 2015-06-19 | 2016-12-22 | Intercept Pharmaceuticals, Inc. | Tgr5 modulators and methods of use thereof |
| MX2018001491A (en) | 2015-08-07 | 2018-04-24 | Intercept Pharmaceuticals Inc | Methods for preparation of bile acids and derivatives thereof. |
| CN105175473B (en) | 2015-08-19 | 2018-12-21 | 丽珠医药集团股份有限公司 | A kind of Austria shellfish cholic acid crystal form I and preparation method thereof, pharmaceutical composition and purposes |
| CN106478759A (en) | 2015-08-31 | 2017-03-08 | 陕西合成药业股份有限公司 | Shellfish chlolic acid derivatives difficult to understand and its production and use |
| CN106518946A (en) | 2015-09-10 | 2017-03-22 | 上海迪诺医药科技有限公司 | Sulfonylurea derivative and pharmaceutical composition and application thereof |
| AU2016325619A1 (en) | 2015-09-24 | 2018-04-12 | Intercept Pharmaceuticals, Inc. | Methods and intermediates for the preparation bile acid derivatives |
| BR112018006892B1 (en) | 2015-10-07 | 2023-04-11 | Intercept Pharmaceuticals, Inc | COMPOUND, PHARMACEUTICAL COMPOSITION AND ITS USES AS FARNESOID X RECEPTOR MODULATORS |
| CN106946867B (en) | 2016-01-06 | 2019-11-12 | 广州市恒诺康医药科技有限公司 | FXR receptor modulators and its preparation method and application |
| CN106995416A (en) | 2016-01-26 | 2017-08-01 | 上海翰森生物医药科技有限公司 | FXR activators and its preparation method and application |
| WO2017128896A1 (en) | 2016-01-26 | 2017-08-03 | 江苏豪森药业集团有限公司 | Fxr agonist and preparation method and use thereof |
| WO2017129125A1 (en) | 2016-01-28 | 2017-08-03 | 正大天晴药业集团股份有限公司 | Steroid derivative fxr agonist |
| CN107021957A (en) | 2016-02-01 | 2017-08-08 | 山东轩竹医药科技有限公司 | FXR receptor stimulating agents |
| WO2017133521A1 (en) | 2016-02-01 | 2017-08-10 | 山东轩竹医药科技有限公司 | Fxr receptor agonist |
| EP3419625B1 (en) | 2016-02-22 | 2021-04-07 | Novartis AG | Methods for using fxr agonists |
| US10323060B2 (en) | 2016-02-23 | 2019-06-18 | Enanta Pharmaceuticals, Inc. | Benzoic acid derivatives of bile acid as FXR/TGR5 agonists and methods of use thereof |
| US10364267B2 (en) | 2016-02-23 | 2019-07-30 | Enanta Pharmaceuticals, Inc. | Deuterated bile acid derivatives as FXR/TGR5 agonists and methods of use thereof |
| US10323061B2 (en) | 2016-02-23 | 2019-06-18 | Enanta Pharmaceuticals, Inc. | Heteroaryl containing bile acid analogs as FXR/TGR5 agonists and methods of use thereof |
| CN108883305B (en) | 2016-03-11 | 2021-03-16 | 英特塞普特医药品公司 | 3-deoxy derivatives and pharmaceutical compositions thereof |
| US10080742B2 (en) | 2016-04-26 | 2018-09-25 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use thereof |
| WO2017189663A1 (en) | 2016-04-26 | 2017-11-02 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as fxr agonists and methods of use thereof |
| WO2017189652A1 (en) | 2016-04-26 | 2017-11-02 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as fxr agonists and methods of use thereof |
| US10138228B2 (en) | 2016-05-18 | 2018-11-27 | Enanta Pharmaceuticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use therof |
| WO2017201155A1 (en) | 2016-05-18 | 2017-11-23 | Enanta Pharmaceuticals, Inc. | lSOXAZOLE DERIVATIVES AS FXR AGONISTS AND METHODS OF USE THEREOF |
| WO2017201150A1 (en) | 2016-05-18 | 2017-11-23 | Enanta Pharmaceuticals, Inc. | Isoxazole analogs as fxr agonists and methods of use thereof |
| AR108711A1 (en) | 2016-06-13 | 2018-09-19 | Gilead Sciences Inc | FXR MODULATING COMPOUNDS (NR1H4) |
| CA2968836C (en) | 2016-06-13 | 2025-09-02 | Gilead Sciences, Inc. | Fxr (nr1h4) modulating compounds |
| JP6678779B2 (en) | 2016-06-13 | 2020-04-08 | ギリアード サイエンシーズ， インコーポレイテッド | FXR (NR1H4) modulating compound |
| TW201808283A (en) | 2016-08-05 | 2018-03-16 | 廣東東陽光藥業有限公司 | Nitrogen-containing tricyclic compounds and uses thereof in medicine |
| JP7093341B2 (en) | 2016-08-23 | 2022-06-29 | アルデリックス， インコーポレイテッド | Hormone receptor regulators for the treatment of metabolic disorders and disorders |
| CN109906223A (en) | 2016-10-04 | 2019-06-18 | 英安塔制药有限公司 | Isoxazole analog is as FXR agonist and its application method |
| CN107973790A (en) | 2016-10-22 | 2018-05-01 | 合帕吉恩治疗公司 | Heterocyclic FXR conditioning agent |
| US10597391B2 (en) | 2016-10-26 | 2020-03-24 | Enanta Pharmaceuticals, Inc. | Urea-containing isoxazole derivatives as FXR agonists and methods of use thereof |
| CN108017636A (en) | 2016-11-04 | 2018-05-11 | 合帕吉恩治疗公司 | Nitrogen-containing heterocycle compound as FXR conditioning agents |
| US11780885B2 (en) | 2016-11-17 | 2023-10-10 | Glaxosmithkline Biologicals Sa | Zika viral antigen constructs |
| CA3045023A1 (en) | 2016-11-29 | 2018-06-07 | Enanta Pharmaceuticals, Inc. | Process for preparation of sulfonylurea bile acid derivatives |
| CN106588804B (en) | 2016-12-09 | 2018-11-09 | 都创(上海)医药科技有限公司 | A kind of preparation method of compound as Farnesoid X receptor (FXR) |
| CN106632294A (en) | 2016-12-15 | 2017-05-10 | 宁波百纳西药业有限公司 | Spiro compound and medicinal use thereof |
| WO2018133730A1 (en) | 2017-01-20 | 2018-07-26 | 四川科伦博泰生物医药股份有限公司 | Heterocyclic compound, preparation method and use therefor |
| CN108341822B (en) | 2017-01-23 | 2021-04-16 | 广州市恒诺康医药科技有限公司 | FXR receptor modulator and preparation method and application thereof |
| US10472386B2 (en) | 2017-02-14 | 2019-11-12 | Enanta Pharmaceuticals, Inc. | Bile acid derivatives as FXR agonists and methods of use thereof |
| US20200131129A1 (en) | 2017-03-15 | 2020-04-30 | Metacrine, Inc. | Farnesoid x receptor agonists and uses thereof |
| JP7136802B2 (en) | 2017-04-07 | 2022-09-13 | エナンタ ファーマシューティカルズ インコーポレイテッド | Process for the preparation of sulfonyl carbamate bile acid derivatives |
| WO2018190643A1 (en) | 2017-04-12 | 2018-10-18 | Il Dong Pharmaceutical Co., Ltd. | An isoxazole derivatives as nuclear receptor agonists and used thereof |
| CN110662743B (en) | 2017-05-26 | 2022-09-30 | 石药集团中奇制药技术（石家庄）有限公司 | Lactam compounds as FXR receptor agonists |
| CA3068928C (en) | 2017-07-06 | 2022-05-31 | Xuanzhu (Hainan) Biopharmaceutical Co., Ltd. | Fxr agonist |
| US10829486B2 (en) | 2018-02-14 | 2020-11-10 | Enanta Pharmacueticals, Inc. | Isoxazole derivatives as FXR agonists and methods of use thereof |
| CN109053751A (en) | 2018-08-30 | 2018-12-21 | 成都海博锐药业有限公司 | FXR regulator with spirane structure |
-
2016
- 2016-03-30 JP JP2017550939A patent/JP6785788B2/en active Active
- 2016-03-30 US US15/085,800 patent/US10457703B2/en active Active
- 2016-03-30 AU AU2016242861A patent/AU2016242861B2/en active Active
- 2016-03-30 WO PCT/US2016/025035 patent/WO2016161003A1/en not_active Ceased
- 2016-03-30 PL PL16774118T patent/PL3277286T3/en unknown
- 2016-03-30 HU HUE16774118A patent/HUE054960T2/en unknown
- 2016-03-30 EP EP16774118.0A patent/EP3277286B1/en active Active
- 2016-03-30 DK DK16774118.0T patent/DK3277286T3/en active
- 2016-03-30 RU RU2017134013A patent/RU2712099C2/en active
- 2016-03-30 SG SG11201707263XA patent/SG11201707263XA/en unknown
- 2016-03-30 MY MYPI2017703433A patent/MY192135A/en unknown
- 2016-03-30 CA CA2981503A patent/CA2981503C/en active Active
- 2016-03-30 CN CN201680020045.2A patent/CN107427527B/en active Active
- 2016-03-30 RS RS20210895A patent/RS62110B1/en unknown
- 2016-03-30 SG SG10201910670RA patent/SG10201910670RA/en unknown
- 2016-03-30 HR HRP20211066TT patent/HRP20211066T1/en unknown
- 2016-03-30 SI SI201631279T patent/SI3277286T1/en unknown
- 2016-03-30 ES ES16774118T patent/ES2886766T3/en active Active
- 2016-03-30 NZ NZ735126A patent/NZ735126A/en unknown
- 2016-03-30 LT LTEP16774118.0T patent/LT3277286T/en unknown
- 2016-03-30 SM SM20210593T patent/SMT202100593T1/en unknown
- 2016-03-30 MX MX2017012558A patent/MX379579B/en unknown
- 2016-03-30 KR KR1020177030546A patent/KR102681304B1/en active Active
- 2016-03-30 PT PT167741180T patent/PT3277286T/en unknown
-
2017
- 2017-09-03 IL IL254288A patent/IL254288B/en active IP Right Grant
- 2017-09-04 PH PH12017501586A patent/PH12017501586A1/en unknown
- 2017-10-24 ZA ZA2017/07212A patent/ZA201707212B/en unknown
-
2019
- 2019-10-04 US US16/593,262 patent/US11040998B2/en active Active
-
2021
- 2021-04-26 ZA ZA2021/02769A patent/ZA202102769B/en unknown
- 2021-05-19 US US17/324,464 patent/US11958879B2/en active Active
- 2021-07-20 CY CY20211100660T patent/CY1124404T1/en unknown
-
2024
- 2024-03-05 US US18/595,487 patent/US20240327452A1/en active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX2017012558A (en) | DERIVATIVES OF BILIAR ACID AS FXR / TGR5 AGONISTS AND METHODS FOR USE. | |
| PH12019550050A1 (en) | Isoxazole analogs as fxr agonists and methods of use thereof | |
| CY1123595T1 (en) | BILE ACID DERIVATIVES AS FXR/TGR5 AGENTS | |
| MX2020004024A (en) | COLANO DERIVATIVES FOR USE IN THE TREATMENT AND/OR PREVENTION OF DISEASES INVOLVED BY FXR AND TGR5/GPBAR1. | |
| MY192717A (en) | Bile acid derivatives as fxr/tgr5 agonists and methods of use thereof | |
| CO2019000386A2 (en) | Heterocyclic compounds as immunomodulators | |
| CY1121413T1 (en) | DIHYDROPYRROLOPYRIDINE ROR-GAMMA INHIBITORS | |
| CR20200312A (en) | NEW PYRIDOPYRIMIDINONES SUBSTITUTED WITH BENZYLAMINE AND DERIVATIVES AS SOS INHIBITORS1 | |
| BR112017009657A2 (en) | bile acid analogues as fxr / tgr5 agonists and methods of using them | |
| DOP2012000257A (en) | DERIVATIVES OF THE ACID 1-AMINO-2-CICLOPROPILETILBORONICO | |
| CU20160188A7 (en) | INDAZOLE COMPOUNDS SUBSTITUTED AS IRAK4 INHIBITORS | |
| EA201691134A1 (en) | NEW GLUTAMINASE INHIBITORS | |
| CL2016002072A1 (en) | 2-amino-3,5,5-trifluoro-3,4,5,6-tetrahydropyridines as bace1 inhibitors for the treatment of Alzheimer's disease | |
| UY33885A (en) | INHIBITION OF IL17 AND IFN-GAMMA FOR THE TREATMENT OF AUTOIMMUNE INFLAMMATIONS | |
| CL2016003214A1 (en) | Indolizine derivatives as phosphoinositide-3 kinase inhibitors | |
| CR20170513A (en) | USEFUL PIRAZOL DERIVATIVES AS INHIBITORS OF 5-LI-POXIGENASA ACTIVATING PROTEIN (FLAP). | |
| PH12016502480A1 (en) | Compounds, pharmaceutical composition and their use in treating neurodegenerative diseases | |
| EA201891690A1 (en) | FXR AGONIST, PRESENTING STEROID DERIVATIVE | |
| CR20190028A (en) | HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS | |
| EA201990686A1 (en) | NAPHTHIRIDINE COMPOUNDS AS JAK KINASE INHIBITORS |